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64269-9910 NDC - BRUISEGUARD MD ()

Drug Information

Product NDC: 64269-9910

Proprietary Name: Bruiseguard MD

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Scarguard Labs, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/1/2009

Package Information

No. Package Code Package Description Billing Unit
164269-9910-47 BLISTER PACK in 1 BOX (64269-9910-4) / 1 KIT in 1 BLISTER PACK

NDC Record

Field Name Field Value Definition
PRODUCT NDC64269-9910The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEBruiseguard MDThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/1/2009This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEScarguard Labs, LLCName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023